Medical Manager

About the role

We are an international specialty pharmaceutical organisation seeking a Medical Manager to provide scientific and medical leadership across our clinical programmes. You will ensure high‑quality study design, execution and oversight while supporting innovative treatments.

Key responsibilities

• Lead medical oversight for clinical studies, including protocol development and Quality‑by‑Design principles.
• Act as medical monitor: safety review, medical queries, and oversight of study conduct.
• Support development of CRFs, Medical Monitoring Plans and Clinical Study Reports.
• Maintain strong relationships with investigators and clinical sites.
• Provide medical input to pharmacovigilance activities for clinical and post‑authorisation studies.
• Review clinical and safety data, identify risks and propose solutions.
• Ensure inspection readiness and support GCP audits/inspections.
• Contribute to process improvements, digital trial initiatives and cross‑functional knowledge transfer.
• Deliver internal scientific training and represent the organisation at scientific meetings.
• Support communication with regulatory authorities as required.

Required profile

• MD (or equivalent) from the UK, EU or USA.
• 3+ years experience in clinical research or clinical development.
• Strong knowledge of ICH/GCP and global clinical trial regulations.
• Experience in medical monitoring, protocol development and clinical data review.
• Excellent written and verbal communication skills.
• Strong analytical, decision‑making and project leadership abilities.
• Ability to work independently, manage deadlines and solve problems quickly.

Required skills

• ICH/GCP compliance
• Quality‑by‑Design (QbD)
• Pharmacovigilance

What we offer

• Competitive salary and benefits.
• Opportunity to impact patient care and contribute to scientific progress.
• High exposure to senior scientific experts and strategic programmes.
• Collaborative, intellectually driven environment focused on clinical excellence.
• Hybrid work model with two days on‑site.